Organolithium-induced alkylative ring opening of aziridines: synthesis of unsaturated amino alcohols and ethers.
Organolithium-induced alkylative ring opening of N-sulfonyl-protected aziridinyl ethers is described. The reactions were efficiently carried out with a variety of organolithiums, providing a promising new strategy to unsaturated amino alcohols and ethers. Cis- and trans-1,4-dimethoxybut-2-ene-derive...
Κύριοι συγγραφείς: | Hodgson, D, Stefane, B, Miles, T, Witherington, J |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2006
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Unsaturated 1,2-amino alcohols and ethers from aziridines and organolithiums.
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Organolithium-induced enantioselective alkylative double ring-opening of epoxides: synthesis of enantioenriched unsaturated amino alcohols
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Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines
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Έκδοση: (2003) -
Unsaturated 1,2-amino alcohols from dihydropyrrole epoxides and organolithiums
ανά: Hodgson, D, κ.ά.
Έκδοση: (2002) -
Enantioselective alkylative double ring opening of epoxides: synthesis of enantioenriched unsaturated diols and amino alcohols.
ανά: Hodgson, D, κ.ά.
Έκδοση: (2002)